GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Echinicola vietnamensis KMM 6221, DSM 17526

Align Spermidine/putrescine import ATP-binding protein PotA, component of The spermidine/putrescine uptake porter, PotABCD (characterized)
to candidate Echvi_2123 Echvi_2123 ABC-type spermidine/putrescine transport systems, ATPase components

Query= TCDB::Q97Q42
         (385 letters)



>FitnessBrowser__Cola:Echvi_2123
          Length = 318

 Score =  174 bits (440), Expect = 4e-48
 Identities = 108/345 (31%), Positives = 193/345 (55%), Gaps = 41/345 (11%)

Query: 6   IEFKNVSKVFEDSNTKVLKDINFELEEGKFYTLLGASGSGKSTILNIIAGLLDATTGDIM 65
           ++   VSK + D+ +  L+D + +++ G   +++G SGSGKS++L IIAGL   + G + 
Sbjct: 4   LKVSEVSKRY-DAGSLALEDFSLQVKRGGVVSMVGESGSGKSSLLRIIAGLEVQSAGVVH 62

Query: 66  LDGVRINDIPTNKR-----DVHTVFQSYALFPHMNVFENVAFPLRLRKIDKKEIEQRVAE 120
           L   +I + P  K      ++  + Q Y L+P+  V EN+A PL L   DK   ++R AE
Sbjct: 63  LGDQKILN-PAQKLVPGYDEIQLIHQEYKLYPNSTVEENIARPLLL--YDKAYQKERTAE 119

Query: 121 VLKMVQLEGYEKRSIRKLSGGQRQRVAIARAIINQPRVVLLDEPLSALDLKLRTDMQYEL 180
           +L+++ L  ++ +  R+LSGGQ+Q+VAI RA+  +P V+LLDEP S+LD   + D+  EL
Sbjct: 120 ILELLSLRAFKDKKPRQLSGGQQQKVAIGRALSIEPEVLLLDEPFSSLDAIQKRDLIEEL 179

Query: 181 RELQQRLGITFVFVTHDQEEALAMSDWIFVMNDGEIVQSGTPVDIYDEPINHFVATFIGE 240
           +E+   L +T +FVTHD ++AL MS+ + ++  G+++Q G   +++ +P + +VA   G 
Sbjct: 180 KEIFDALEVTVIFVTHDVDDALLMSEELLIIQKGKLLQQGNVREVFRKPASAYVARLFGY 239

Query: 241 SNILPGTMIEDYLVEFNGKRFEAVDGGMKPNEPVEVVIRPEDLRITLPEEGKLQVKVDTQ 300
            N++PG                            E  +RP +++IT   +  ++ +V  Q
Sbjct: 240 LNLIPGA--------------------------EEAYVRPSEVKIT--SKTSIKAEVVKQ 271

Query: 301 LFRGVHYEIIAYDELGNE--WMIHSTRKAI-VGEEIGLDFEPEDI 342
            F  +HY ++      +E  W +    +++ VG+E+ LD++ E +
Sbjct: 272 QFL-IHYNLLTVKLEDSELFWKVDDPSRSVNVGDEVFLDYQKEQL 315


Lambda     K      H
   0.318    0.138    0.386 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 295
Number of extensions: 19
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 385
Length of database: 318
Length adjustment: 29
Effective length of query: 356
Effective length of database: 289
Effective search space:   102884
Effective search space used:   102884
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory